| Drug NDC: | 43742-0292 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. | |
| Proprietary Name: | Enviro Ii |
| Also known as the trade name. It is the name of the product chosen by the labeler. | |
| Proprietary Name Base: | Enviro |
| The base of the Brand/Proprietary name excluding its suffix. | |
| Proprietary Name Suffix: | II |
| A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard. | |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. | |
| Non Proprietary Name: | Potassium Gluconate, Glandula Suprarenalis Suis, Hepar Suis, Canary Feathers, Standardized Cat Hair, Cattle Epithelia, Chicken Feathers, Dog Epithelia, Duck Feathers, Gerbil Epithelia, Goat Epithelia, Goose Feathers, Guinea Pig Epithelia, Hamster Epithelia, Hog Epithelia, Horse Epithelia, Mouse Epithelia, Parakeet Feathers, Rabbit Epithelia, Rat Epithelia, House, Mattress, Rug, Upholstery, Barley, Corn, Oat, Wheat, Rice, Millet, Milo, Dust Mite, Alfalfa, Golden Rod (solidago Virguarea), Red Clover |
| Also known as the generic name, this is usually the active ingredient(s) of the product. | |
| Labeler Name: | Deseret Biologicals |
| Name of Company corresponding to the labeler code segment of the ProductNDC. | |
| Dosage Form: | Liquid |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. | |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. | |
| Substance Name: | ACER NEGUNDO POLLEN - 9 [hp_X]/mL AGROSTIS GIGANTEA POLLEN - 9 [hp_X]/mL ALFALFA - 9 [hp_X]/mL AMBROSIA ACANTHICARPA POLLEN - 9 [hp_X]/mL AMBROSIA ARTEMISIIFOLIA - 9 [hp_X]/mL AMBROSIA PSILOSTACHYA POLLEN - 9 [hp_X]/mL AMBROSIA TRIFIDA POLLEN - 9 [hp_X]/mL ANAS PLATYRHYNCHOS FEATHER - 9 [hp_X]/mL ANSER ANSER FEATHER - 9 [hp_X]/mL ARSENIC TRIOXIDE - 12 [hp_X]/mL Load more... BARLEY - 9 [hp_X]/mL BETULA OCCIDENTALIS POLLEN - 9 [hp_X]/mL BOS TAURUS SKIN - 9 [hp_X]/mL BROWN RICE - 9 [hp_X]/mL CANIS LUPUS FAMILIARIS SKIN - 9 [hp_X]/mL CAPRA HIRCUS SKIN - 9 [hp_X]/mL CARYA OVATA POLLEN - 9 [hp_X]/mL CAVIA PORCELLUS SKIN - 9 [hp_X]/mL CORN GRAIN - 9 [hp_X]/mL DACTYLIS GLOMERATA TOP - 9 [hp_X]/mL DERMATOPHAGOIDES FARINAE - 9 [hp_X]/mL EQUUS CABALLUS SKIN - 9 [hp_X]/mL FAGUS GRANDIFOLIA POLLEN - 9 [hp_X]/mL FELIS CATUS HAIR - 9 [hp_X]/mL FRAXINUS AMERICANA POLLEN - 9 [hp_X]/mL GALLUS GALLUS FEATHER - 9 [hp_X]/mL HISTAMINE DIHYDROCHLORIDE - 30 [hp_X]/mL HOUSE DUST - 9 [hp_X]/mL HYALURONIDASE - 30 [hp_X]/mL INTERFERON .GAMMA. PORCINE RECOMBINANT - 30 [hp_X]/mL IRIDIUM - 12 [hp_X]/mL JUGLANS NIGRA POLLEN - 9 [hp_X]/mL MELOPSITTACUS UNDULATUS FEATHER - 9 [hp_X]/mL MERIONES UNGUICULATUS SKIN - 9 [hp_X]/mL MESOCRICETUS AURATUS SKIN - 9 [hp_X]/mL MILLET - 9 [hp_X]/mL MUS MUSCULUS SKIN - 9 [hp_X]/mL OAT - 9 [hp_X]/mL ORYCTOLAGUS CUNICULUS SKIN - 9 [hp_X]/mL PHLEUM PRATENSE TOP - 9 [hp_X]/mL PHOSPHORUS - 12 [hp_X]/mL PLATANUS OCCIDENTALIS POLLEN - 9 [hp_X]/mL POA PRATENSIS TOP - 9 [hp_X]/mL POPULUS DELTOIDES SUBSP. DELTOIDES POLLEN - 9 [hp_X]/mL PORK LIVER - 8 [hp_X]/mL POTASSIUM GLUCONATE - 6 [hp_X]/mL QUERCUS RUBRA POLLEN - 9 [hp_X]/mL RATTUS NORVEGICUS SKIN - 9 [hp_X]/mL RUMEX ACETOSELLA POLLEN - 9 [hp_X]/mL RUMEX CRISPUS TOP - 9 [hp_X]/mL SALIX NIGRA POLLEN - 9 [hp_X]/mL SELENIUM - 12 [hp_X]/mL SERINUS CANARIA FEATHER - 9 [hp_X]/mL SEROTONIN HYDROCHLORIDE - 30 [hp_X]/mL SOLIDAGO VIRGAUREA FLOWERING TOP - 9 [hp_X]/mL SORGHUM BICOLOR WHOLE - 9 [hp_X]/mL SULFUR - 12 [hp_X]/mL SUS SCROFA ADRENAL GLAND - 8 [hp_X]/mL SUS SCROFA SKIN - 9 [hp_X]/mL TRIFOLIUM PRATENSE FLOWER - 9 [hp_X]/mL ULMUS AMERICANA POLLEN - 9 [hp_X]/mL WHEAT - 9 [hp_X]/mL |
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. | |
| Route Details: | ORAL |
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. | |
| Marketing Start Date: | 23 Sep, 2013 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. | |
| Marketing End Date: | 30 Jan, 2024 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. | |
| Listing Expiration Date: | 12 Jun, 2026 |
| This is the date when the listing record will expire if not updated or certified by the firm. | |
| Manufacturer Name: | Deseret Biologicals |
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. | |
| Original Packager: | Yes |
| Whether or not the drug has been repackaged for distribution. | |
| NUI: | N0000185367 N0000175629 N0000184306 N0000185001 M0017130 M0000728 N0000185006 N0000185373 M0008280 N0000185371 M0006342 N0000185016 N0000185364 N0000185377 N0000185375 M0016962 N0000185005 M0419493 M0028968 N0000185003 M0576325 M0515971 N0000185374 M0006896 N0000175531 M0009499 |
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). | |
| UNII: | P6K070AR8V HU8V6E7HOA DJO934BRBD U2AI3H2J5Y 9W34L2CQ9A RX18M46K8L KU1V1898XX 83B65P4796 15XI414745 S7V92P67HO Load more... 5PWM7YLI7R R889N2L976 7J12CD6O9L 659G217HPG X2W7CLE97T JLG9853E2P 54UN9R2798 GM3H4U6QS8 C1Z9U7094Z J41552QKAK PR9U2YPF3Q 88VZV9HGT4 34X886W1H4 1564HD0N96 G684LX721Q 1FCM16V0FV 3POA0Q644U EYO007VX98 8KOG53Z5EM 69404B0LO7 44448S9773 1BV28146ZR 1XY644QKWG 9WN2H714TG 3K873H631W TJR6B3R47P 390AN9GB09 Z6J799EAJK Z91WAU43WC S7PW24BX20 27YLU75U4W E03U1K03LK 7EA48700V9 476DVV63WP 6EC706HI7F 12H3K5QKN9 SVW19ET93C Y69HPD48AI N52MIQ81ZW S9T422Q956 6M2JIH93ZN H6241UJ22B 9EL3384IQY GKN429M9VS 5405K23S50 Y3T98X3AL6 70FD1KFU70 398IYQ16YV 3EM4VW6TQN 4JS0838828 89BAT511BD 4J2I0SN84Y |
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. | |
| Pharmacologic Class EPC: | Non-Standardized Pollen Allergenic Extract [EPC] Standardized Pollen Allergenic Extract [EPC] Non-Standardized Feather Allergenic Extract [EPC] Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Animal Skin Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [EPC] Standardized Insect Allergenic Extract [EPC] Standardized Animal Hair Allergenic Extract [EPC] Non-Standardized House Dust Allergenic Extract [EPC] Endoglycosidase [EPC] |
| Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`. | |
| Pharmacologic Class PE: | Increased Histamine Release [PE] Cell-mediated Immunity [PE] Increased IgG Production [PE] |
| Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`. | |
| Pharmacologic Class CS: | Pollen [CS] Allergens [CS] Feathers [CS] Dietary Proteins [CS] Plant Proteins [CS] Antigens, Dermatophagoides [CS] Insect Proteins [CS] Dander [CS] Salivary Proteins and Peptides [CS] House Dust [CS] Glycoside Hydrolases [CS] |
| Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient]. | |
| Pharmacologic Class: | Allergens [CS] Antigens Dermatophagoides [CS] Cell-mediated Immunity [PE] Cells Epidermal [EXT] Dander [CS] Dietary Proteins [CS] Endoglycosidase [EPC] Feathers [CS] Glycoside Hydrolases [CS] Grain Proteins [EXT] House Dust [CS] Increased Histamine Release [PE] Increased IgG Production [PE] |
| These are the reported pharmacological class categories corresponding to the SubstanceNames listed above. | |
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|---|---|---|---|
| 43742-0292-1 | 30 mL in 1 BOTTLE, DROPPER (43742-0292-1) | 23 Sep, 2013 | 30 Jan, 2024 | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. | ||||
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